Stefanos Kachris
Research Subjects
Stefanos Kachris has a total of 12 co-authors. Here are the top co-authors by number of shared publications:
- Chara Papadaki
Laboratory of Translational Oncology, School of Medicine, University of Crete, 71500 Heraklion, Greece
2 shared publications - Christoforos Nikolaou
Biomedical Sciences Research Center "Alexander Fleming
2 shared publications Chrysanthi Kokkinaki
2 shared publicationsEliza Tsitoura
2 shared publicationsGeorge Sourvinos
2 shared publicationsKonstantinos Rounis
2 shared publications
Latest Publications
- 6 January 2025
- Published by Elsevier in Physica Medica
- Vol. 130, 104896
A qualitative, quantitative and dosimetric evaluation of a machine learning-based automatic segmentation method in treatment planning for gastric cancer
- 6 January 2025
- Published by Elsevier in Physica Medica
- Vol. 130, 104896
A qualitative, quantitative and dosimetric evaluation of a machine learning-based automatic segmentation method in treatment planning for gastric cancer
- Open Access
- 1 February 2022
- Published by Taylor & Francis in Cancer Management and Research
- Vol. ume 14, 409-410
Circulating miRNAs as Potential Biomarkers in Prostate Cancer Patients Undergoing Radiotherapy [Corrigendum]
Corrigendum for the article Circulating miRNAs as Potential Biomarkers in Prostate Cancer Patients Undergoing Radiotherapy
- 1 February 2022
- Published by Taylor & Francis in Cancer Management and Research
- Vol. ume 14, 409-410
Open AccessCirculating miRNAs as Potential Biomarkers in Prostate Cancer Patients Undergoing Radiotherapy [Corrigendum]
Corrigendum for the article Circulating miRNAs as Potential Biomarkers in Prostate Cancer Patients Undergoing Radiotherapy
- Open Access
- 1 November 2021
- Published by Taylor & Francis in Cancer Management and Research
- Vol. ume 13, 8257-8271
Circulating miRNAs as Potential Biomarkers in Prostate Cancer Patients Undergoing Radiotherapy
Introduction: Disease recurrence is a major concern in patients with localized prostate cancer (PCa) following treatment with radiotherapy (RT), and few studies have evaluated the clinical relevance of microRNAs (miRNAs) prior and post-RT. Purpose: We aimed to investigate the significance of miRNAs in the outcomes of prostate cancer patients undergoing radiotherapy and to identify the related pathways through bioinformatics analysis. Materials and Methods: The expression levels of miR-21, miR-106b, miR-141 and miR-375 involved in the response to radiotherapy were assessed by RT-qPCR in the serum of PCa patients (n=56) prior- and post-RT. Results: Low expression levels of miR-106b prior-RT were associated with extracapsular extension and seminal vesicles invasion by the tumor (p=0.031 and 0.044, respectively). In the high-risk subgroup (n=47), post-RT expression levels of miR-21 were higher in patients with biochemical relapse (BR) compared to non-relapse (p=0.043). Also, in the salvage treatment subgroup (post-operative BR; n=20), post-RT expression levels of miR-21 and miR-106b were higher in patients with BR compared to non-relapse (p=0.043 and p=0.032, respectively). In the whole group of patients, high expression levels of miR-21 prior-RT and of miR-106b post-RT were associated with significantly shorter overall survival (OS; p=0.049 and p=0.050, respectively). No associations were observed among miR-141 and miR-375 expression levels with clinicopathological features or treatment outcome. Bioinformatics analysis revealed significant enrichment in DNA damage response pathways. Conclusion: Circulating miRNAs prior or post-RT may hold prognostic implications in patients with PCa.
- 1 November 2021
- Published by Taylor & Francis in Cancer Management and Research
- Vol. ume 13, 8257-8271
Open AccessCirculating miRNAs as Potential Biomarkers in Prostate Cancer Patients Undergoing Radiotherapy
Introduction: Disease recurrence is a major concern in patients with localized prostate cancer (PCa) following treatment with radiotherapy (RT), and few studies have evaluated the clinical relevance of microRNAs (miRNAs) prior and post-RT. Purpose: We aimed to investigate the significance of miRNAs in the outcomes of prostate cancer patients undergoing radiotherapy and to identify the related pathways through bioinformatics analysis. Materials and Methods: The expression levels of miR-21, miR-106b, miR-141 and miR-375 involved in the response to radiotherapy were assessed by RT-qPCR in the serum of PCa patients (n=56) prior- and post-RT. Results: Low expression levels of miR-106b prior-RT were associated with extracapsular extension and seminal vesicles invasion by the tumor (p=0.031 and 0.044, respectively). In the high-risk subgroup (n=47), post-RT expression levels of miR-21 were higher in patients with biochemical relapse (BR) compared to non-relapse (p=0.043). Also, in the salvage treatment subgroup (post-operative BR; n=20), post-RT expression levels of miR-21 and miR-106b were higher in patients with BR compared to non-relapse (p=0.043 and p=0.032, respectively). In the whole group of patients, high expression levels of miR-21 prior-RT and of miR-106b post-RT were associated with significantly shorter overall survival (OS; p=0.049 and p=0.050, respectively). No associations were observed among miR-141 and miR-375 expression levels with clinicopathological features or treatment outcome. Bioinformatics analysis revealed significant enrichment in DNA damage response pathways. Conclusion: Circulating miRNAs prior or post-RT may hold prognostic implications in patients with PCa.